- Research article
- Open Access
Identification of stress-responsive genes in Ammopiptanthus mongolicususing ESTs generated from cold- and drought-stressed seedlings
© Liu et al.; licensee BioMed Central Ltd. 2013
- Received: 16 November 2012
- Accepted: 25 May 2013
- Published: 5 June 2013
Ammopiptanthus mongolicus is the only evergreen broadleaf shrub in the northwest desert of China, which can survive long-term aridity and extremely cold environments. In order to understand the genetic mechanisms underlying stress tolerance and adaptation to unfavorable environments of woody plants, an EST approach was used to investigate expression patterns of A. mongolicus in response to abiotic stresses.
ESTs were generated from a cDNA library constructed from A. mongolicus seedlings subjected to cold and drought stresses. Analysis of 5,637 cDNA sequences led to the identification of 5,282 ESTs and 1,594 unigenes, which were denoted as the AmCDUnigene set. Of these, 70% of unigenes were annotated and classified into 12 functional categories according to Gene Ontology, and 30% of unigenes encoded unknown function proteins, suggesting some of them were novel or A. mongolicus specific genes. Using comparative analysis with the reported genes from other plants, 528 (33%) unigenes were identified as stress-responsive genes. The functional classification of the 528 genes showed that a majority of them are associated with scavenging reactive oxygen species, stress response, cellular transport, signal transduction and transcription. To further identify candidate abiotic stress-tolerance genes, the 528 stress-responsive genes were compared with reported abiotic stress genes in the Comparative Stress Genes Catalog of GCP. This comparative analysis identified 120 abiotic stress-responsive genes, and their expression in A. mongolicus seedlings under cold or drought stress were characterized by qRT-PCR. Significantly, 82 genes responded to cold and/or drought stress. These cold- and/or drought-inducible genes confirmed that the ROS network, signal transduction and osmolyte accumulation undergo transcriptional reorganization when exposed to cold or drought stress treatments. Additionally, among the 1,594 unigenes sequences, 155 simple sequence repeats (SSRs) were identified.
This study represents a comprehensive analysis of cold and/or drought stress-responsive transcriptiome of A. mongolicus. The newly characterized genes and gene-derived markers from the AmCDUnigene set are valuable resources for a better understanding of the mechanisms that govern stress tolerance in A. mongolicus and other related species. Certain up-regulated genes characterizing these processes are potential targets for breeding for cold and/or drought tolerance of woody plants.
- Ammopiptanthus mongolicus
- Cold tolerance
- Differential expression
- Drought tolerance
- Expressed sequence tags
- Stress-responsive genes
Environmental degradation, especially desertification, has become a serious problem due to the world’s population increases, the extensive agricultural practices and the effects of the global climate changes. The proliferation of woody plants in arid and high latitude deserts is essential for sustainable conservation and amelioration of environments. Genetic improvement of forest trees for tolerance to environmental stresses such as drought, high salinity, low temperature and heat is a promising approach for the future of environmental conservation. It is vital to know how plants respond to environmental stresses and which biochemical pathways and genes are involved in stress tolerance. To date, numerous physiological and biochemical traits have been observed, and hundreds of underlying genes have been characterized according to the recent developments in functional genomics of some herbaceous model plants such as Arabidopsis[1, 2] and rice [3, 4]. However, molecular mechanisms by which woody plants respond to abiotic stresses remain poorly understood despite their biological and practical importance.
The genus Ammopiptanthus (Leguminosae), endemic to the eastern desert of Central Asia, includes two species: A. mongolicus (Maxim.) Cheng f. and A. nanus (M. Pop.) Cheng f. . Ammopiptanthus is the only genus of evergreen broadleaf shrub in the northwest desert of China and both species are dominant in the local vegetation, so this genus plays an important role in fixing moving sands and delaying further desertification. The biological property of Ammopiptanthus evergreen broadleaf has been viewed as an ancestral trait that identifies it as a Tertiary relict taxon . The vegetation in northwest China was dominated by evergreen and/or deciduous broadleaf forests in the early Tertiary period according to the fossil evidence . When subsequent changes made the climate colder and drier from the early Miocene (24–16 Ma) in Central Asia , the forests were gradually replaced by steppe and then by desert . Today, their habitats are stony and/or sandy deserts where the climate is arid (annual precipitation ranges from 100–160 mm) and the temperature varies from below -30°C in the winter to +40°C in the summer. Because of low seed germination rates in the harsh environments and increasing anthropogenic pressures in their natural range, both A. mongolicus and A. nanus have been categorized as ‘endangered’ species. As a relict survivor of the evergreen broadleaf forest in this region from the Tertiary period, Ammopiptanthus has acquired the strong ability to adapt to the dry and extremely cold environments. The specificities above have recently attracted scientific attention to their anatomy , cold and drought stress resistance [11–13], and genetic diversity and geographic differentiation [14, 15]. However, little genome information has been reported in regard to its resistance mechanisms to environmental stresses, despite this genotype with strong tolerances making A. mongolicus an excellent species to study cold and drought tolerance.
Understanding a plant’s response to a stress will require a global analysis of stress-responsive genes. A significant insight into the expressed portion of a plant with a large size and unknown genome is through large-scale generation and analysis of expressed sequence tags (ESTs). cDNA libraries prepared from different tissues exposed to various stress conditions are valuable tools to obtain the expressed and stress-regulated portion of the genome. This not only leads to the identification of genes that have known or putative functions, but also to the discovery of novel, previously unknown putative genes. Recent studies have demonstrated that the EST approach has been successfully used to discover novel genes and to investigate expression patterns of woody plants in response to abiotic stresses, such as the expression profile of Tamarix androssowii in response to NaHCO3 stress , ESTs of apple (Malus x domestica ‘Royal Gala’) in response to low temperature and water deficit , ESTs of poplar leaves subjected to multiple abiotic stresses , and ESTs from cold-acclimated and non-acclimated leaves of Rhododendron catawbiense Michx . In the present study, more than 5,000 ESTs were generated from A. mongolicus seedlings after cold and drought stress treatments, allowing construction of an AmCDUnigene (A. mongolicus cold and drought stress unigenes) set of 1,594 putative genes. These data offer a valuable genomic resource to study cold-acclimation and drought adaptation in A. mongolicus, and to identify key genes in regulation of cold and drought tolerance in this plant.
The quality of the cDNA Library
Since we aimed to identify both early and late cold-responsive and/or drought-responsive genes through EST analysis, a cDNA library, AmCDL (A. mongolicus cold- and drought-responsive library), was constructed from pooled samples of A. mongolicus seedlings at different stages of cold treatment and water deficit. Blue/white plaque selection following incubation of an aliquot of the library showed a 95.5% recombinant rate with titers of 1.01×106. Insert length was evaluated with 96-randomly selected representative clones by PCR amplification and sequencing before large-scale sequencing. According to the sequencing data, the mean size of the insert cDNAs was 0.8 kb. The full length ratio of the 96 sequenced clones was 57.4% by BLAST searching the 5’end sequences in GenBank.
Generation and analysis of ESTs
The main objective of this study was to produce collections of EST sequences and cDNA clones in order to discover abotic stress-responsive or abiotic stress-tolerance genes in A. mongolicus. Bacterial clones were randomly picked from the library and 6,240 (65×96) single pass sequence reactions (IDs SDQ001_A01 to SDQ065_H12) were performed on cDNAs present in plasmid from their 5′ ends of these clones (Table 1). Thus, this cDNA library generated 5,282 high quality ESTs of 100 bp or longer, with an average sequence length of 681.6 bp. The sequence lengths of more than one half (55%) of the ESTs are above 700 bp with the longest sequence being 865 bp (Figure 1). Based on homology searching, 3,741 (70.8%) sequences matched their homologs in the NCBI sequence (non-redundant nucleotide or protein) databases, and 57.5% (3,064) of these inserts represented full-coding lengths (Table 1) based on comparative BLAST analysis.
The 5,282 ESTs were clustered into 461 contigs and 1,145 singletons, giving 1,606 candidate genes (Table 1). After removing rRNA, mitochondrial, chloroplast sequences, and some redundant sequences, the candidate gene set consisted of 1,594 unigenes with an average length of 720 bp and the longest unigene of 1,713 bp (Figure 1). These final genes were denoted as the AmCDUnigene (A. mongolicus cold and drought stress unigenes) set.
General characteristics of A. mongolicus ESTs, showing number of ESTs in each category
Total number of readable sequences obtained
Vector sequence, low quality and other contaminants
Sequences below 100bp
High quality ESTs
Full-length ratio of ESTs (Percentage)
ESTs matching to Nr database (Percentage)
Unigenes matching to Nr database (Percentage)
Annotation and functional classification
The annotation of the AmCDUnigene set was based on sequence homology. Each gene in the unigene set inherited the annotation from the best match found after a BLASTX search against the NCBI protein database. Search results revealed that 70.4% of the unigenes had hits with known putative functions, and the remaining 29.6% showed some homology with no characterized function such as unknown proteins, hypothetical proteins, etc. As the ESTs in this study were obtained from a cDNA library constructed from cold- and drought-stressed A. mongolicus seedlings, it is possible that some of these 29.6% unigenes were involved in the cold- and/or drought-stress response and/or are unique genes in A. mongolicus, though they may be expressed at varied levels under non-stress conditions. However, validation of their function will be the focus of our future studies.
prevalent GOSlim categories were that of cellular metabolism (11.48%), followed by protein biosynthesis (7.28%) and electron transport (6.71%), suggesting a high degree of basic metabolic activity in the stressed tissues. Less prevalent GOSlim categories were those of response to stress (5.40%), signal transduction (5.96%), transcription (5.58%) and transport (5.83%). These GO categories have been implicated in the general stress response pathways consisting of stress recognition, downstream signaling events, defense and adaptation responses.
The best matched species
BLASTN searches. Similarly, more than one half (57%) had best hits from the sequences of legume (including Glycine max, Medicago truncatula, Lotus japonicus, Pisum sativum and Arachis hypogaea etc.) in BLASTN searches and less than one quarter had hits in BLASTX searches. This is reasonable for the legume woody plant A. mongolicus considering the bias of codon usage.
The most abundant ESTs
Apart from providing an efficient method for gene discovery, EST data sets can be used to provide low precision estimates of mRNA levels through estimations of EST redundancy. In this study, the redundancy of specific genes was worked out according to the results of the 5′ annotation (Table 2) with the best homolog match from a BLASTX search against the NCBI protein database. Of the 461 contigs from the AmCDL library, 13 contigs in the 20 most highly represented transcripts encode photosynthetic-related proteins, such as ribulose 1, 5-bisphosphate carboxylase/oxygenase small chain (650 clones), chlorophyll a/b binding proteins (265 clones for type I and 156 clones for type II), plastocyanin (142 clones), and photosystem reaction center subunits (Table 2). The other abundant transcripts included metallothionein type 2 (134 clones), lipid transfer protein-like protein (70 clones), auxin-repressed protein, carbonic anhydrase, and ferredoxin-1.
ESTs abundance was further analyzed based on the classification of corresponding unigenes. Less than 4% photosynthetic genes were derived from 28% ESTs. Electron transport genes (6.71%, Figure 3) were also abundant according to the ESTs classification percentage (6.17%). This category included multiple electron transport genes that were involved in radical scavenging or detoxification, such as the abundant transcripts of metallothioneins, ferredoxins and thioredoxins.
Identification of stress-responsive genes
Putative function of the 20 most abundant sequences in cold- and drought-treated A. mongolicus seedlings
Number of ESTs
small subunit rbcS1
Chlorophyll a/b-binding protein type I
Chlorophyll a/b binding protein type II
Metallothionein type 2
Chloroplast photosystem II PsbR
Lipid transfer protein-like protein
Photosystem I reaction center subunit XI
Glycine cleavage system T protein
Photosystem I reaction center subunit X
Chloroplast oxygen-evolving enhancer protein
/oxygenase activase alpha 2
Photosystem I psaH protein
Photosystem I reaction center subunit III
according to the earlier GO categories, but the functions of other genes involved in stress responses remain to be determined. Comparative in silico analyses of all A. mongolicus unigenes with those in other plants led to the identification of a putative function for 528 stress-responsive genes. These genes account for 33% of the total unigenes and 30% of the ESTs, which were classified into 12 functional groups (Figure 5) based on similar functional characteristics, cellular roles or their involvement in cellular processes or pathways. The list of the 528 stress-responsive genes identified from our ESTs, along with the annotation and GO category is presented as supplementary file, see Additional file 1.
Additionally, to ascertain whether these stress-responsive genes were involved in the response to cold or drought stress in A. mongolicus, we compared these stress-responsive genes with previously reported abiotic stress genes from other organisms documented in the Comparative Stress Genes Catalog of GCP (Generation Challenge Programme, http://www.generationcp.org). This web site has compiled a comparative crop stress gene catalog with available information of four plant abiotic stresses (cold, salt, ABA and drought). Surprisingly, only 120 abiotic stress-responsive genes were found in 78 families in the Catalog (Additional file 2: Table S1, Additional file 3). These genes were involved in the ROS scavenging, signaling cascades, transport, membrane composition, photosynthesis, transcription regulation and protective functions. Interestingly, 90% of families (50/55) were identified as drought-responsive genes and only five of them were cold-responsive (Additional file 3), except for 23 families whose stress types were not shown in the Catalog. More genes responded to drought than cold, indicating that drought-responsive genes were dominant in cold- and/or drought-stressed A. mongolicus. Furthermore, the EST number of the 120 (7.5%) contigs account for 16.6% of the total ESTs, suggesting the abundance of these genes in A.mongolicus. Multiple abundant genes with more than ten ESTs were present in these genes, including 6 of the top 20 most abundant unique sequences (Table 2, Additional file 2: Table S1). They mainly participate in the photosynthesis and oxidoreduction pathways.
Differential expression of cold- or drought-inducible genes in A. mongolicus
To further characterize abiotic stress-responsive genes listed in Additional file 3 as cold- and/or drought-inducible genes identified in A. mongolicus, the expression pattern of the 120 genes under cold and drought conditions were analyzed by qRT-PCR. Relative transcription values of 97 genes were obtained (Additonal file 3). Their fold changes in expression of the treatments relative to that of the control at each time point were color coded and shown in Additional file 2: Table S1. Some uniscripts with abundant ESTs in Table 2 were noted for being highly expressed as shown in Additonal file 3, which confirmed the quantitative EST results. It was obvious that many of the uniscripts had strongly enhanced expression under cold and/or drought conditions; however, the differences in the response pattern between the two treatments were striking, suggesting that these genes may play different roles in A. mongolicus under the two types of stresses. Despite several attempts using different primer pairs, we could not obtain reproductive expression patterns of 23 transcripts, thus they were shown as blank in Additional file 3.
The qRT-PCR results confirmed that 85% of the abiotic stress-responsive genes (82 of the 97 detected uniscripts) were cold- or drought-inducible in A. mongolicus. Most of these inducible genes (76 of 82) were up-regulated under the cold condition. Less than half (47, 48%) of these detected genes were up-regulated under the drought condition. Moreover, compared with 35 unigenes expressed specifically under cold treatment, only 7 genes were expressed uniquely under drought treatment. More genes appeared cold-inducible than drought-inducible in A. mongolicus, which is not consistent with the display of stress type in the Catalog. These inconsistencies may be attributed to the biological differences among plant species used, stress treatment conditions, their response to abiotic stresses, and/or detection methodologies. Since more cold-inducible genes were found in this study, it may be suggest that cold stress or low temperature is a more severe limiting factor for A. mongolicus.
Among these stress-induced genes, we found that five genes showing significant induction (≥8 fold) in at least one time point during cold or drought stress were well known stress-inducible genes, including NAC domain protein gene (AM0328), actin depolymerizing factor gene (AM0262), beta-amylase gene (AM0598), low temperature and salt responsive protein gene (AM0047), and ubiquitin-conjugating enzyme E2 gene (AM0976). Several transcripts displayed exclusive or predominant stress specificity, for example GTP binding protein RAB1D gene (AM0790) and actin depolymerizing factor gene (AM0262) for drought stress, but NAC domain protein gene (AM0328), desiccation protectant protein Lea14 gene (AM1436), low temperature and salt responsive protein gene (AM0047) and chloroplast Cu/Zn SOD gene (AM0701) for cold stress. Little is known about the function of these genes under cold and/or drought stresses in A. mongolicus, though some genes were found responsive to abiotic stress in other species. The action mode of these genes in A. mongolicus will be further studied in our lab.
Identification and characterization of SSRs
A set of 1594 unigenes sequences, comprising a total of 1.13 Mb of sequence, was searched for SSRs with a repeat motif length ranging from two to six nucleotides using SSIT. In total, 155 di- to hexa- nucleotide SSRs were identified from 138 (8.7%) unigenes (Additional file 4), with an average of one SSR per 7.2 kb. Of those, 16 (11.6%) genes contained more than one SSR. Analysis of these SSR motifs revealed that the proportion of SSR unit sizes was not evenly distributed. Most of these satellites are di- or tri- nucleotide motifs, being 36 (23.2%) and 76 (49%). The occurrences of tetra- to hexa-nucleotides were 19 (12.3%), 9 (5.8%) and 15 (9.7%), respectively. The AG/CT was the most frequent repeat motif and accounted for 10.3% (16/155), followed by AAG/CTT (7.7%, 12/155), AGA/TCT (7.7%, 12/155), GAA/TTC (6.4%, 10/155) and AG/CT (5.8%, 9/155). Most of the tetra- to hexa-nucleotide motifs were found only once. The mean SSR length of each unit varied between 14 and 30 bp. The overall average of SSR length was 19 bp with a maximum of 36 bp hexa-nucleotide repeat (AACCCA).
Table 3 shows the type and position of SSRs in the gene sequences. The majority (68%, 105/155) of the identified SSRs are present in the untranslated regions (UTRs), including all dinucleotide, tetrancleotide and pentanucleotide repeats. Trinucleotide (57%, 43/76) and hexanucleotide (47%, 7/15) repeats, causing no frame-shift, are mainly found in the coding regions. In contrast, repeat motifs containing di-, tetra- and pentanucleotides, resulting in frame shifts when undergoing slip-strand mutations, were primarily found in untranslated regions, and rare in ORFs. And SSRs in the 5′ UTR (71) are more frequent than in the 3′ UTR (23).
Additionally, among the 138 unigenes containing SSRs, 53 (38%) were stress-responsive genes and 37 (27%) were unknown. These stress-responsive genes include ten proteins that participate in radical scavenging, such as thioredoxin, cytochrome C reductase, glutaredoxin and peroxiredoxin, etc., five signal transduction proteins (SOS2, calmodulin, serine/threonine phosphatase, etc.), nine stress-responsive proteins (dehydrins, stress enhanced protein, cold acclimation responsive protein and defensin), nine transcription factors, four heat stress proteins and secondary metabolism proteins, etc.. The most frequent motifs contained in these stress-responsive genes were AAG/CTT, AG/CT and AGA/TCT. Interestingly, more than one half of SSRs were present in the 5′UTR of the 53 stress-responsive genes, one third within ORFs and only five in the 3′UTR.
ESTs have proven to be a valuable tool for gene discovery and a number of EST collections from many different plants are now publicly available according to the Expressed Sequence Tags Database in NCBI (http://www.ncbi.nlm.nih.gov/dbEST). In A. mongolicus, an ideal plant for investigating the cold and drought resistance mechanisms of the woody plants endemic to the desert of northwestern China, only hundreds of ESTs have been sequenced and a small number of sequences from cold- or drought-treated seedlings are available in the NCBI databases despite a recent report on a transcriptomic study with PEG-treated roots of this species . Therefore there is a great need for developing more ESTs on abiotic stress genes of this shrub. In this study, we obtained 5,282 sequences from cold- and drought-treated seedlings of A. mongolicus, giving 1,594 unigenes. Since we are interested in all the genes involved in abiotic stresses, leaves treated from short term (1 h) to long term (8 d) were pooled for cDNA construction and EST generation. Molecular functional classification of the 1,594 unigenes shows a large number of genes that are predicted to be involved in electron transport, response to stress, signal transduction and regulation of transcription. Using comparative analysis of stress-responsive genes from other plants, 528 (33% of total unigenes) (Additional file 1) putative stress genes were identified in the AmCDUnigene set. By comparing the 528 stress-responsive genes with reported abiotic stress genes from other organisms in the Comparative Stress Genes Catalog of GCP, 120 abiotic stress-responsive genes in A. mongolicus seedlings were identified, and their transcriptional patterns under cold and drought stresses were characterized by qRT-PCR. Eighty-five percent of detected genes (82 of 97 detected genes) were found cold- or drought-inducible, confirming the AmCDUnigene data in some cases. These genes could be involved in multiple pathways, such as the reactive oxygen species network, photosynthesis, stress response, transcriptional regulation, signal transduction, etc., which probably all participate in stress tolerance improvement of A. mongolicus. The putative functions of these pathways and involved genes during cold and drought responses are discussed later.
Distribution of SSRs with respect to putative open reading frames (ORFs)
chain, chlorophyll a/b binding protein, plastocyanin, photosystem reaction center proteins, and carbonic anhydrase. Some of them were identified as cold and/or drought stress genes (Additional file 2: Table S1). The qRT-PCR results in Additional file 2: Table S1 and Additional file 3 confirmed their abundance and responses to the stresses.
The over-representation of ESTs encoding chlorophyll a/b binding proteins (156 ESTs for type II and 265 ESTs for type I CARCAB1) and their high expression levels and up-regulation detected by qRT-PCR (AM0022 and AM0084 in Additional file 2: Table S1 and Additional file 3) under the cold conditions suggest their participation of cold tolerance of A. mongolicus. The enzymes ribulose-1,5-bisphosphate carboxylase/oxygenase activases (AM0042) were also found highly transcribed and up-regulated in cold-treated seedlings (Additional file 2: Table S1 and Additional file 3). Carbonic anhydrase, which is known to maintain optimal CO2 concentrations , may be thus helping to efficiently use the CO2 and available light energy under cold and drought conditions. Expression changes of these genes may reflect their involvement in the stress acclimation of A. mongolicus.
Low temperature and water deficit disrupt photosynthesis and increase photorespiration and thus cause an increased production of reactive oxygen species (ROS). ROS accumulation in stress cells must be kept tightly under control by an efficient and versatile scavenging system to avoid damage and cell death. In the cold- and drought-stressed seedlings of A. mongolicus, a battery of scavenging enzymes genes were present, including multiple superoxide dismutases (SODs), thioredoxins (Trxs), ferredoxins (Frxs), glutaredoxins (Grxs), peroxiredoxins (PrxRs), metallothioneins (Mts), ascorbate peroxidases (APXs), catalase (CAT), glutathione peroxidases (GPXs), etc., all of which may be involved in the ROS network of acclimation and stress response.
In chloroplasts, not only SODs, but PrxRs and Trxs can provide antioxidative protection for detoxification of photochemically produced H2O2 and play an important role during drought and oxidative stress [23, 24]. Trx and Grx are ubiquitous disulfide reductases that regulate the redox status of target proteins, such as peroxiredoxins ; GPX display peroxidase activity preferentially in the presence of Trx [26, 27]. Trxs also interact through a disulfide bridge with SODs and germin-like proteins [28, 29], as well as Frxs . Frx and Grx function in maintaining the reduced state of antioxidants ascorbic acid and glutathione . Additionally, Mts are ubiquitous Cys-rich proteins known to be involved in ROS scavenging [32, 33]. The regeneration of Mts after oxidative modification may involve endogenous dithiols, such as Trx . Up-regulation (Additional file 2: Table S1) and abundance of these scavengers in the AmCDUnigene set and the reported above interaction between them indicate the complex and redundant ROS scavenging pathways, which may play a central role in the consequent regulation of acclimation and stress tolerance in cold- and drought-treated A. mongolicus seedlings.
Molecular signals and their roles in transcription
A general stress signal transduction pathway starts with signal perception, followed by the generation of second messengers, which modulate intracellular Ca2+ levels, often initiating a protein phosphorylation cascade that finally targets proteins directly involved in transcription factors controlling specific sets of stress-regulated genes . Our data showed that multiple genes were present in the AmCDUnigene set encoding proteins involved in stress signaling cascades, such as different types of protein kinases and phosphatases, Ca2+ messenger system proteins as well as GTP binding proteins and ethylene signaling protein. The expression data in Additional file 2: Table S1 showed that GTP binding protein gene (AM1171), calmodulin gene (AM0287) and calcium-dependent protein kinase CDPK gene (AM0463) were greatly increased under both cold and drought conditions, reflecting the multiplicity of cold and drought stress signals in A. mongolicus.
The potentially increased activities of various signaling pathways are associated with differential expression of many families of transcriptional factors. The functional class of the transcription associated genes comprised families of transcriptional factors including multiple types of zinc finger proteins (such as C3HC4, C2H2, GATA and AN1), MYB, NAC domain proteins, bZIP transcription factors, AP2 domain-containing transcription factors, and bHLH transcription factors. Several members of these families were previously identified as being responsive to various stresses , such as the AP2 family to cold and drought, bZIP to drought and ABA, MYB to dehydration, zinc finger to cold and drought, bHLH and NAC to drought, salinity and ABA. Similar results were obtained in cold- and drought-stressed A. mongolicus in which expression of NAC domain protein gene (AM0328) and ethylene response factor gene (AM1353) were significantly up-regulated (Additional file 2: Table S1). An important and noteworthy observation was that zinc finger, bZIP and MYB transcription regulators showed predominance in this plant. Though the most studied members are those of the AP2/ERF family, which had previously shown to be the regulators of the majority of cold- and drought-responsive genes, only three contigs encoding ERF, DREB and TINY-like protein were found in this AmCDUnigene set belonging to this family.
Cellular transport and homeostasis
Stress-induced reorganization and spatial distribution of many key metabolites in plants require efficient transport machinery. Water transport is of great importance to water homeostasis in plants under cold and drought stresses. Up-regulated transcription of aquaporin and membrane intrinsic proteins in A. mongolicus, like in a number of other plant species , may act as a major player to respond to cold or drought stress. The role of nutrients such as nitrogen and phosphorus on cold hardiness has received attention because low temperatures not only limit nitrification , but also inhibit photosynthesis and consequently reduce inorganic phosphate availability . The increased transcription of amino acid transporter (AM1518) and phosphate transporter (AM1013) during cold and drought treatments may indicate a readjustment of the cellular Pi and N status for reestablishing cell nutrient homeostasis in A. mongolicus.
It was reported that dehydration and cold stress induced sugar transporters in Arabidopsis and sugarcane , which may be a response to an increased demand for carbohydrates to protect cells under stress conditions. The non-specific lipid transfer proteins were also reported to respond to drought and in some cases to cold [42, 43] by facilitating the transfer of phospholipids, glycolipids, fatty acids and steroids between membranes. Overexpression of one member of the ABC-transporters improved drought and salt stress resistance in Arabidopsis. Various transport-associated genes were found in this study, encoding ABC-transporters, non-specific lipid-transfer proteins, sugar transporters, metal transporter, phosphate transporter and nitrate transporter, which may constitute the transport machinery of A. mongolicus under cold and drought conditions.
Cellular processes like translation, post-translational events and protein degradation are crucial for cell survival under varied environmental conditions. In the present study, these classes constituted about 15% of the unigenes and 8.9% of ESTs and comprised predominantly of the ribosomal protein genes and heat stress protein genes apart from proteinase genes and ubiquitin genes. Genes encoding multiple ribosomal protein subunits, multiple protein translation initiation factors, and translation elongation factors were all found in this AmCDUnigene set. These proteins play a pivotal role in translation and their presence in the set indicates they play a role in stress response of A. mongolicus.
Ubiquitin and proteasome-mediated protein degradation plays a crucial role in enabling plants to alter their proteome to maximize their chances of survival under various circumstances . Expression data (Additional file 2: Table S1) showed six ubiquitin-conjugating enzymes were all significantly up-regulated in A. mongolicus during cold and drought stresses, suggesting their involvement in stress tolerance of this plant.
It is well established that molecular chaperones, often called heat shock proteins, are critical for cell survival in times of stress to ensure proper folding of protein substrate, protein disaggregation and protein degradation. Five of six major families of heat shock protein genes in plant are presented in this AmCDUnigene set, including Hsp70 family (DnaK/Ssa), J-protein/Hsp40 family (DnaJ/Ydj1), Hsp90 family, Hsp100 (caseino-lytic proteinases, Clp) family and small Hsp family (sHsp). A current model for sHsp function proposes that they protect thermo-sensitive substrates from irreversible heat stress-induced denaturation and aggregation . J-proteins not only play a crucial role in maintaining the protein homeostasis by reestablishing functionally native conformations but are involved in stress signaling pathways during various abiotic stresses . The major functions of Hsp70 were also multiple, such as preventing aggregation, assisting refolding, protein import, signal transduction and transcription activation . The transcription of these Hsps/chaperaones and improved transcription of Hsp70s (AM0676 and AM0734) and Hsp90 (AM0898) (Additional file 2: Table S1) suggest that similar protein protection mechanisms exist in A. mongolicus.
Some genes that are involved in carbohydrate metabolism and up-regulated under stress conditions in other plants were also found up-regulated in cold- and/or drought-stressed A. mongolicus (Additional file 2: Table S1). Most of these genes regulate starch and sugar metabolism and may participate in the protection of macromolecules in cells from damage. For instance, beta-amylase, which has a primary role to produce maltose during hydrolytic starch degradation and was up-regulated under cold conditions  in Arabidopsis, was significantly up-regulated under both cold and drought conditions in A. mongolicus. The expression of trehalose-phosphatase/synthase (AM1068) was increased according to qRT-PCR assay as presented in Additional file 2: Table S1, indicating its involvement in drought stress tolerance of A. mongolicus. Similar results were reported in transgenic Arabidopsis where overexpressing AtTPS1 (trehalose-6-P synthase) displayed a dehydration tolerance phenotype , and AtTPS5 was also found in the involvement of stress tolerance .
Plant responses to stress
The AmCDUnigene set represents a rich source of stress-responsive A. mongolicus genes and presented multiple dehydration-responsive protein genes, late embryogenesis abundant (LEA) protein genes, and cold-regulated protein genes. Usually, dehydration-responsive protein genes respond to drought and cold-regulated protein genes express under cold, though some of them respond to more than one stress. For instance, desiccation protectant protein Lea14 (AM1436) is up-regulated not only under drought but also cold stress, which is similar with other LEA protein genes accumulating in vegetative tissues exposed to dehydration, osmotic, and low temperature stress [52, 53]. LEA proteins have been proposed to stabilize membranes and prevent crystallization of cellular components due to their extreme stability and hydrophilicity . The uningene (AM0047) encoded a protein that is similar to hydrophobic protein RCI2A (RARE-COLD-INDUCIBLE 2A), also known as low temperature and salt responsive protein, and its expression was highly promoted by cold and drought treatments. In general, RCI2 genes could be induced by ABA and abiotic stress, and were potentially involved in the regulation of plasma membrane potential . The up-regulated LEA and RCI2A in A. mongolicus may illuminate their participation in cell protection and rescue processes.
Defense-related genes encoding proteinase inhibitors, plant defensins, disease resistance proteins and chitinases were found in the AmCDUnigene set. Many disease resistance protein genes have shown to be expressed in response to abiotic stresses , but their exact role remains unknown. The chitinase genes are also up-regulated by abiotic stress such as drought , and by ethylene and jasmonic acid , though their biological role under drought remains unclear. Jasmonic acid was reported to significantly affect expression of drought-related genes, indicating that there is extensive cross-talk between responses to drought and other environmental factors including biotic stresses . The presence of these defense response genes in A. mongolicus implicates their involvement in abiotic response besides their key role in pathogen stress.
About 30% of the 1594 unigenes genes were identified with unknown functions. These were divided into two groups, one in which homologous or similar genes from other organism exist and one where no significant similarities could be found to any other sequence, i.e. genes that could be A. mongolicus-specific. Assuming that many of these 471 A. mongolicus-specific unknown genes are cold- and/or drought-related, some new abiotic stress genes may be present in this collection. Such genes are potentially interesting and could encode unknown proteins or regulatory factors that need to be characterized to discover new pathways and mechanisms adapted by plants to cope with abiotic stresses. A study is necessary for the 471 genes to elucidate which A. mongolicus-specific unknown genes are responsive to cold or drought stress.
SSRs derived from ESTs essentially represent expressed genetic sequences and hence are potential candidates for the construction of markers for gene tagging and comparative genomic studies . In this study we found trinucleotide repeats to be the most common SSR type in ESTs of A. mongolicus. This is in agreement with a majority of studies that report trinucleotide repeats were the most abundant class of SSRs in A. mongolicus sequences  and in other plant ESTs . Interestingly, more than one half of known unigenes that contain SSRs were stress-responsive genes with SSRs present in the 5′UTR or within ORFs, which indicated that these SSRs may be involved in regulating expression of these genes or enhancing protein functions. The exact function for these SSR-containing stress genes and how they occurred need to be further characterized. Thus, characterization of these stress-responsive genes and gene-based functional markers may provide a shortcut to illuminating the mechanism of stress tolerance requirement in A. mongolicus.
The AmCDUnigene set containing 1,594 genes was generated from a cDNA library constructed from A. mongolicus seedlings subjected to cold and drought stresses. Of these, 30% of unigenes encoded unknown function proteins and 70% of unigenes were annotated and classified into 12 broad functional categories. Further analysis revealed that 528 (33%) unigenes had similarity to genes known to be involved in stress responses in other plant species such as ROS scavenging, cellular transport, signal transduction and transcription processes. By comparing the 528 stress-responsive genes with reported abiotic stress genes in the Comparative Stress Genes Catalog of GCP, 120 abiotic stress-responsive genes in A. mongolicus seedlings were identified. Transcriptional analysis showed that 82 genes were cold- or drought-inducible, confirming that ROS network, signal transduction and osmolyte accumulation undergo transcriptional reorganization when exposed to cold or drought stress. Additionally, 155 SSRs were found in the 1,594 unigene sequences.
This study represents an exploration of molecular responses of A. mongolicus seedlings to cold and drought stresses using trancriptomic analysis. Together, the abiotic stress-responsive ESTs and the subsequent gene expression analysis provide a large number of excellent candidate genes for future investigation into the adaptation of A. monglicus in adverse conditions. However, a better understanding of the biological function of those stress-responsive genes and the genetic mechanisms underlying the stress tolerance of A. mongolicus would be anticipated in the future studies using an integrated approach involving physiological evaluation and experimental validation. In addition, the genomic resources and advanced knowledge developed from this study will contribute to efficient breeding of new trees and ornamental woody plants with improvement in abiotic stress tolerance.
Plant materials and growth conditions
Two-week-old A. mongolicus seedlings were used in this work. Seeds were obtained from an experimental forest farm in Dengkou of Bayannaoer in Inner-Mongolia of China. The seeds were germinated in pots with water-saturated medium and maintained in growth conditions of 60% relative humidity under an illumination of 200 μmol m-2 sec-1 and a 14-hour photoperiod with 26°C during the day and 22°C during the night. Cold treatments were performed by incubating the seedlings at 4-6°C for 1 h, 2 h, 4 h, 8 h, 24 h, 48 h, 96 h and 8 d, then the aerial parts were sampled at each time point and pooled. For water deficit treatment, seeds were sown in the same medium to germinate in growth conditions as described above, and then no water was added to the medium. It was the fifth day when 80% of the seedlings were wilting (seedlings showing 50-60% relative water content and medium showing 50% field capacity) due to lack of water. Samples were harvested at the last four days (i.e., the 12th, 13th, 14th and 15th days after sowing seeds) of the 15-day drought treatment period, respectively (50-70% field capacity). Seedlings of A.mongolicus prepared similarly but without any treatment served as the control (CK) in this study.
RNA isolation, cDNA library construction and EST sequencing
The samples of every time point were pooled in equal amounts. Total RNA was extracted from the pooled seedlings as described by Chang et al. with some modifications. Frozen tissues were ground to a fine powder in liquid nitrogen, transferred to 68°C CTAB extraction buffer, and extracted twice with phenol:chloroform (1:1) in equal volumes. RNA was precipitated overnight at 4°C with 2M lithium chloride. The precipitate was dissolved in 0.5% SDS, extracted with an equal volume of chloroform, precipitated with two volumes ethanol, and re-suspended in DEPC-treated water. Poly(A)+ mRNA was isolated from total RNA using the Oligotex Direct mRNA kit (Qiagen, Valencia, CA, USA) according to manufacturer’s instructions and was quantified spectrophotometrically at OD260.
The cDNA library was created using SMART™ cDNA Library Construction Kit (Clontech, Palo Alto, CA, USA). The SMART™IV Oligonucleotide was used in the first-strand synthesis to generate a high yield of full-length, double-stranded cDNA. Synthesized cDNA was digested with asymmetrical SfiI restriction enzyme sites at the 5′ and 3′ cDNA ends and ligated into SfiI-digested vector pBluescript II SK, which was modified and contains the asymmetrical SfiI sites in the MCS and facilitates directional cloning. White clones grown on screening LB medium (Amp/IPTG/X-Gal) were recovered by random colony selection and inserts were sequenced from the 5′ end using T7 primer and an ABI 3730 capillary sequencer in Shanghai United Gene Institute of China.
Sequence processing and analysis
Standard sequence processing tools, Phred , Phrap and Cross_match [64, 65], were used with Codoncode InterPhace (http://www.codoncode.com). The vector sequence, low-complexity, repeats, poly (A) and low quality regions present at the beginning and end of each sequence were trimmed using Phred 20 cutoff value. Vector screening was performed using the Cross_match program with Codoncode InterPhace software. Sequences were edited for the removal of rRNA, mitochondrial DNA and other contaminants. In the next step, PHRAP was used to assemble the individual ESTs into clusters of sequences derived from the same transcript to reduce the redundancy of the dataset and increase the overall quality of the derived consensus sequences. The criterion setting for clustering sequences together was an alignment of a minimum of 100 bases and with at least 90% similarity between the aligned sequences. Sequences that did not fit into a contig were defined as singletons. Finally, ESTs in singletons that had passed the filters and unmasked sequences < 100 bases were discarded. The resulting singletons and contigs represented the AmCD (A. mongolicus cold and drought) candidate gene set.
Function annotation and classification
Various genomic tools were used to identify annotated sequences. Homology searches were performed against non-redundant nucleotide and protein sequence databases using BLASTN 2.2.12 and BLASTX 2.2.12 versions of the BLAST programs through BLAST 2.0 network client software. The accession numbers and E-value of the best matches were extracted from the result files. If two or more query sequences resulted in best matches with identical accession numbers, they were sorted according to their E-values. Only the sequence with the lowest E-value was included in the unigene set. The unigenes were annotated based on the results of BLASTX searches of the non-redundant database. The definition line of the BLAST match was used as a description of the putative function of the unigene. An E-value threshold of 1e-10 was used and unigenes that did not meet this requirement were annotated as unknown. Assigning GO (Gene Ontology) category to each of the unigenes was based on this annotation.
Identification of genes associated with abiotic stress
The genes associated with stress responses were identified from multiple sources, based on the complied list of stress-regulated genes documented in various plant species (http://stress-genomics.org). Data from microarray expression profiles and ESTs of possible abiotic stress genes in Arabidopsis[1, 2, 48], rice [3, 4, 66], barley  and other plants [40, 68] were also used. The unigenes were also compared with those abiotic stress response genes in other organisms reported by the GCP (Generation Challenge Programme) at the Comparative Stress Genes Catalog website (http://dayhoff.generationcp.org) for candidate abiotic stress genes in A. mongolicus. The accession numbers in UniProt of the best BLASTX matches with E-value < 1e-10 were used to search in the Comparative Stress Genes Catalog.
Quantitative real-time PCR (qRT-PCR)
The candidate abiotic stress genes from ESTs were validated by performing qRT-PCR at each of the 4 time points of cold treatment (1 d, 2 d, 4 d and 8 d), drought treatment (12th, 13th, 14th and 15th days after sowing, which were referred as 1 d, 2 d, 3 d and 4 d of treatment) and control, respectively. Total RNA from each time point and control were treated with RNase-free DNase to remove residue DNA. Two micrograms of total RNA were reverse-transcribed using 1 μL 50 μM oligo (dT)20 and 200 units of SuperScriptTM III Reverse Transcriptase (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s instructions. Triplicate qRT-PCR reactions were performed in 384-well plates with ABI PRISM7900HT Real-Time PCR System (Applied Biosystems, CA, USA) using the SYBR R Premix Ex Taq TM kit (Takara, Japan), forward and reverse (final concentration 0.2 μM) primers and 100 ng cDNA template. The cycling program was: 95°C for 30 s, 40 cycles of 95°C for 5 s and 60°C for 34 s. PCR primers were designed using Primer Premiers 5.0 and had a primer length of 20–24 nucleotides, a GC content of 40-60% and an optimal annealing temperature of 58 to 60°C, with amplicon lengths between 100 and 250 bp. Triplicate measurements were averaged and the mean value was used for further calculations. Melting curve analysis was performed after PCR to evaluate the presence of any nonspecific PCR products and primer dimers. Genes relative transcription levels were normalized to the geometric mean of two EIF (eukaryotic translation factor) genes, eIF1 (JN885965) and eIF3 (JN885967) . The fold change for a particular target was determined by comparing the relative transcription value of the treatment with that of the control. A statistical cut-off, P <0.05, was used to determine which genes were differentially expressed. The probe sets and the corresponding primer pairs used for the analysis are listed in Additional file 5.
Identification of SSRs and open reading frame
The tool of SSRIT (Simple Sequence Repeat Identification Tool) online (http://www.gramene.org/db/markers/ssrtool)  was used to search for SSRs (simple sequence repeats) with a repeat motif length of two to six nucleotides sequences in the 1,594 candidate genes set. The minimum repeat unit was defined as seven for di-nucleotides, five for tri-nucleotides and four for tetra-, penta-, and hexa-nucleotides, according to previously described by Bräutigam et al.. Compound SSRs were defined as ≥ 2 SSRs interrupted by ≤ 50 bases .
To predict the position of SSRs with respect to coding regions, the open reading frames (ORFs) were identified. ORF prediction was based on BLASTX hits and ORF finder tools (http://www.ncbi.nlm.nih.gov/gorf/orfig.cgi). The part of the ORF that matched the best BLASTX hit was considered as seed to select the right coding region from the six frame translations provided by ORF finder. Based on the both results, we defined the beginning and the end of the ORF. Usually an open reading frame starts with an ATG (methionine) and ends with a stop codon (TAA, TAG or TGA).
The sequencing data have been submitted to the dbEST of GenBank under the accession numbers of JZ356671 - JZ356878, JZ388729 –JZ389985 and the library accession number of LIBEST_028198, Ammopiptanthus mongolicus cold- and drought-responsive library.
This work was financially supported by the National Natural Science Foundation of China (Grant No.30700559 to MQL).
- Seki M, Narusaka M, Ishida J, Nanjo T, Fujita M, Oono Y, Kamiya A, Nakajima M, Enju A, Sakurai T, Satou M, Akiyama K, Taji T, Yamaguchi-Shinozaki K, Carninci P, Kawai J, Hayashizaki Y, Shinozaki K: Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J. 2002, 31: 279-292. 10.1046/j.1365-313X.2002.01359.x.PubMedView ArticleGoogle Scholar
- Kreps JA, Wu Y, Chang HS, Zhu T, Wang X, Harper JF: Transcriptome changes for Arabidopsis in response to salt, osmotic, and cold stress. Plant Physiol. 2002, 230: 2129-2141.View ArticleGoogle Scholar
- Rabbani MA, Maruyama K, Abe H, Khan MA, Katsura K, Ito Y, Yoshiwara K, Seki M, Shinozaki K, Yamaguchi-Shinozaki K: Monitoring expression profiles of rice genes under cold, drought, and high salinity stresses and abscisic acid application using cDNA microarray and RNA gel-blot analyses. Plant Physiol. 2003, 133: 1755-1767. 10.1104/pp.103.025742.PubMedPubMed CentralView ArticleGoogle Scholar
- Gorantla M, Babu PR, Lachagari VBR, Reddy AMM, Wusirika R, Bennetzen JL, Reddy AR: Identification of stress-responsive genes in an indica rice (Oryza sativa L.) using ESTs generated from drought-stressed seedlings. J Exp Bot. 2007, 58: 253-265.PubMedView ArticleGoogle Scholar
- Cheng SH: Ammopiptanthus Cheng f. A new genus of Leguminosae from central Asia. Journal of Botany USSR. 1959, 44: 1381-1386.Google Scholar
- Liu JQ, Qiu MX, Yang K, Shi QH: Studies on the plant community of Ammopiptanthus mongolicus. Journal of Desert Research. 1995, 15: 109-115.Google Scholar
- Geng BY, Tao JR, Xie GP: Early Tertiary fossil plants and paleoclimate of Lanzhou Basin. Acta Phytaxonomica Sinica. 2001, 39: 105-115.Google Scholar
- Guo ZT, Ruddiman WF, Hao QZ, Wu HB, Qiao YS, Zhu RX, Peng SZ, Wei JJ, Yuan BY, Liu TS: Onset of Asian desertification by 22 Myr ago inferred from loess deposits in China. Nature. 2002, 416: 159-163. 10.1038/416159a.PubMedView ArticleGoogle Scholar
- Yan S, Mu GJ, Xu YQ: Quaternary environmental evolution of the Lop Nur region, NW China. Acta Micropalaeontologica Sinica. 2000, 17: 165-169.Google Scholar
- Liu JQ, Qiu MX: Ecological, physiological and anatomical traits of Ammopiptanthus mongolicus grown in desert of China. Acta Botanica Sinica. 1982, 24: 568-574.Google Scholar
- Wang W, Wei L: Purification of Boiling-Soluble Antifreeze Protein from the Legume Ammopiptanthus mongolicus. Prep Biochem Biotechnol. 2003, 33: 67-80. 10.1081/PB-120018370.PubMedView ArticleGoogle Scholar
- Liu M, Shen X, Yin W, Lu C: Functional analysis of cold-inducible cDNA clones in the Legume Ammpiptanthus mongolicus. CryoLetters. 2005, 26: 213-222.PubMedGoogle Scholar
- Xu S, An L, Feng H, Wang X, Li X: The seasonal effects of water stress on Ammopiptanthus mongolicus in a desert environment. Journal of Arid Environment. 2002, 51: 437-447. 10.1006/jare.2001.0949.View ArticleGoogle Scholar
- Chen G, Huang H, Kang M, Ge X: Development and characterization of microsatellite markers for an endangered shrub, Ammopiptanthus mongolicus (Leguminosae) and cross-species amplification in Ammopiptanthus nanus. Conserv Genet. 2007, 8: 1495-1497. 10.1007/s10592-007-9306-2.View ArticleGoogle Scholar
- Ge X, Yu Y, Yuan Y, Huang H, Yan C: Genetic Diversity and Geographic Differentiation in Endangered Ammopiptanthus (Leguminosae) Populations in Desert Regions of Northwest China as Revealed by ISSR Analysis. Ann Bot. 2005, 95: 843-851. 10.1093/aob/mci089.PubMedPubMed CentralView ArticleGoogle Scholar
- Wang Y, Yang C, Liu G, Jiang J, Wu J: Generation and analysis of expressed sequence tags from a cDNA library of Tamarix androssowii. Plant Sci. 2006, 170: 28-36. 10.1016/j.plantsci.2005.07.027.View ArticleGoogle Scholar
- Wisniewskia M, Bassetta C, Norellia J, Macarisina D, Artlipa T, Gasicb K, Korban S: Expressed sequence tag analysis of the response of apple (Malus x domestica ‘Royal Gala’) to low temperature and water deficit. Physiol Plant. 2008, 133: 298-317. 10.1111/j.1399-3054.2008.01063.x.View ArticleGoogle Scholar
- Nanjo T, Rutamura N, Nishiguchi M, Igasaki T, Shinozaki K, Shinohara K: Characterization of full length enriched expressed sequence tags of stress-treated poplar leaves. Plant Cell Physiol. 2004, 45: 1738-1748. 10.1093/pcp/pci009.PubMedView ArticleGoogle Scholar
- Wei H, Dhanaraj AL, Rowland LJ, Fu Y, Krebs SL, Arora R: Comparative analysis of expressed sequence tags from cold-acclimated and non-acclimated leaves of Rhododendron catawbiense Michx. Planta. 2005, 221: 406-416. 10.1007/s00425-004-1440-1.PubMedView ArticleGoogle Scholar
- Zhou Y, Gao F, Liu R, Feng J, Li H: De novo sequencing and analysis of root transcriptome using 454 pyrosequencing to discover putative genes associated with drought tolerance in Ammopiptanthus mongolicus. BMC Genomics. 2012, 13: 266-278. 10.1186/1471-2164-13-266.PubMedPubMed CentralView ArticleGoogle Scholar
- Makino A, Sakashita H, Hidema J, Mae T, Ojima K, Osmond B: Distinctive responses of ribulose-1,5-bisphosphate carboxylase and carbonic anhydrase in wheat leaves to nitrogen nutrition and their possible relationships to CO2 transfer resistance. Plant Physiol. 1992, 100: 1737-1743. 10.1104/pp.100.4.1737.PubMedPubMed CentralView ArticleGoogle Scholar
- Dietz KJ, Jacob S, Oelze ML, Laxa M, Tognetti V, de Miranda SM, Baier M, Finkemeier I: The function of peroxiredoxins in plant organelle redox metabolism. J Exp Bot. 2006, 57: 1697-1709. 10.1093/jxb/erj160.PubMedView ArticleGoogle Scholar
- Rey P, Cuine S, Eymery F, Garin J, Court M, Jacquot JP, Rouhier N, Broin M: Analysis of the proteins targeted by CDSP32, a plastidic thioredoxin participating in oxidative stress responses. Plant J. 2005, 41: 31-42.PubMedView ArticleGoogle Scholar
- Santos CVD, Rey P: Plant thioredoxins are key actors in the oxidative stress response. Trends in Plant Sciences. 2006, 11: 329-334. 10.1016/j.tplants.2006.05.005.View ArticleGoogle Scholar
- Wood ZA, Schröder E, Harris JR, Poole LB: Structure, mechanisms and regulation of peroxiredoxins. Trends Biochem Sci. 2003, 28: 32-40. 10.1016/S0968-0004(02)00003-8.PubMedView ArticleGoogle Scholar
- Herbette S, Lenne C, Leblanc N, Julien JL, Drevet JR, Roeckel-Drevet P: Two GPX-like proteins from Lycopersicon esculentum and Helisnthus annuus are antioxidant enzymes with phospholipid hydroperoxides glutathione peroxidase and thioredoxin peroxidase activities. Eur J Biochem. 2002, 269: 2414-2420. 10.1046/j.1432-1033.2002.02905.x.PubMedView ArticleGoogle Scholar
- Jung BG, Lee KO, Lee SS, Chi YH, Jang HH, Kang SS, Lee K, Lim D, Yoon SC, Yun DJ, Inoue Y, Cho MJ, Lee SY: A chinese cabbage cDNA with high sequence identity to phospholipids hydroperoxide glutathione peroxidases encode a novel isoform of thioredoxin-dependent peroxidase. J Biol Chem. 2002, 277: 12572-12578. 10.1074/jbc.M110791200.PubMedView ArticleGoogle Scholar
- Yamazaki D, Motohashi K, Kasama T, Hara Y, Hisabori T: Target proteins of the cytosolic thioredoxins in Arabidopsis thaliana. Plant Cell Physiol. 2004, 45: 18-27. 10.1093/pcp/pch019.PubMedView ArticleGoogle Scholar
- Balmer Y, Vensel WH, Tanaka CK, Hurkman WJ, Gelhaye E, Rouhier N, Jacquot JP, Manieri W, Schürmann P, Droux M, Buchanan BB: Thioredoxin links redox to the regulation of fundamental processes of plant mitochondria. Proc Natl Acad Sci USA. 2004, 101: 2642-2647. 10.1073/pnas.0308583101.PubMedPubMed CentralView ArticleGoogle Scholar
- Pfannschmidt T: Chloroplast redox signals: how photosynthesis control its own genes. Trends Plant Sci. 2003, 8: 33-41.PubMedView ArticleGoogle Scholar
- Mittler R, Vanderauwera S, Gollery M, Van Breusegem F: Reactive oxygen gene network of plants. Trends Plant Sci. 2004, 9: 490-498. 10.1016/j.tplants.2004.08.009.PubMedView ArticleGoogle Scholar
- Wong HL, Sakamoto T, Kawasaki T, Umemura K, Shimamoto K: Down-Regulation of Metallothionein, a Reactive Oxygen Scavenger, by the Small GTPase OsRac1 in Rice. Plant Physiol. 2004, 135: 1447-1456. 10.1104/pp.103.036384.PubMedPubMed CentralView ArticleGoogle Scholar
- Akashi K, Nishimura N, Ishida Y, Yokota A: Potent hydroxyl radical-scavenging activity of drought-induced type-2 metallothionein in wild watermelon. Biochem Biophys Res Commun. 2004, 323: 72-78. 10.1016/j.bbrc.2004.08.056.PubMedView ArticleGoogle Scholar
- Fabisiak JP, Borisenko GG, Liu SX, Tyurin VA, Pitt BR, Kagan VE: Redox sensor function of metallothioneins. Methods Enzymol. 2002, 353: 268-281.PubMedView ArticleGoogle Scholar
- Xiong L, Schumaker KS, Zhu JK: Cell signaling during cold, drought, and salt stress. The Plant Cell. 2002, 14: S165-S183. 10.1105/tpc.010278.PubMedPubMed CentralView ArticleGoogle Scholar
- Shameer K, Ambika S, Varghese SM, Karaba N, Udayakumar M, Sowdhamini R: STIFDB-Arabidopsis Stress Responsive Transcription Factor DataBase. International Journal of Plant Genomics. 2009, 2009: 583429.PubMedPubMed CentralView ArticleGoogle Scholar
- Forrest KL, Bhave M: Major intrinsic proteins (MIPs) in plants: a complex gene family with major impacts on plant phenotype. Funct Integr Genomics. 2007, 7: 263-289. 10.1007/s10142-007-0049-4.PubMedView ArticleGoogle Scholar
- Raven JA, Wollenweber B, Handley LH: Ammonia and ammonium fluxes between photolithotrophs and the environment in relation to the global nitrogen cycle. New Phytol. 1992, 121: 5-18. 10.1111/j.1469-8137.1992.tb01087.x.View ArticleGoogle Scholar
- Hurry V, Strand A, Furbank R, Stitt M: The role of inorganic phosphate in the development of freezing tolerance and the acclimatization of photosynthesis to low temperature is revealed by the pho mutant of Arabidopsis thaliana. Plant J. 2000, 24: 383-396. 10.1046/j.1365-313x.2000.00888.x.PubMedView ArticleGoogle Scholar
- Kiyosue T, Abe H, Yamaguchi-Shinozaki K, Shinozaki K: ERD6, A cDNA clone from an early dehydrateion-induced gene of Arabidopsis, encodes a putative sugar transporter. Biochim Biophys Acta. 1998, 1370: 187-191. 10.1016/S0005-2736(98)00007-8.PubMedView ArticleGoogle Scholar
- Nogueira FTS, De Rosa VE Jr, Menossi M, Ulian EC, Arruda P: RNA expression profiles and data mining of sugarcane response to low temperature. Plant Physiol. 2003, 132: 1811-1824. 10.1104/pp.102.017483.PubMedPubMed CentralView ArticleGoogle Scholar
- García-Olmedo F, Molina A, Segura A, Moreno M: The defensive role of nonspecific lipid-transfer proteins in plants. Trends Microbiol. 1995, 3: 72-74. 10.1016/S0966-842X(00)88879-4.PubMedView ArticleGoogle Scholar
- White AJ, Dunn MA, Brown K, Hughes MA: Comparative analysis of genomic sequence and expression of a lipid transfer protein gene family in winter barley. J Exp Bot. 1994, 45: 1885-1892. 10.1093/jxb/45.12.1885.View ArticleGoogle Scholar
- Kim DY, Jin JY, Alejandro S, Martinoia E, Lee Y: Overexpression of AtABCG36 improves drought and salt stress resistance in Arabidopsis. Physiol Plant. 2010, 139: 170-180. 10.1111/j.1399-3054.2010.01353.x.PubMedView ArticleGoogle Scholar
- Dreher K, Callis J: Ubiquitin, Hormones and Biotic Stress in Plants. Ann Bot. 2007, 99: 787-822. 10.1093/aob/mcl255.PubMedPubMed CentralView ArticleGoogle Scholar
- Siddique M, Gernhard S, Koskull-Döring P, Vierling E, Scharf KD: The plant sHSP superfamily: five new members in Arabidopsis thaliana with unexpected properties. Cell Stress Chaperones. 2008, 13: 183-197. 10.1007/s12192-008-0032-6.PubMedPubMed CentralView ArticleGoogle Scholar
- Rajan VBV, D’Silva P: Arabidopsis thaliana J-class heat shock proteins: cellular stress sensors. Funct Integr Genomics. 2009, 9: 433-446. 10.1007/s10142-009-0132-0.PubMedView ArticleGoogle Scholar
- Wang W, Vinocur B, Shoseyov O, Altman A: Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004, 9: 244-252. 10.1016/j.tplants.2004.03.006.PubMedView ArticleGoogle Scholar
- Seki M, Narusaka M, Abe H, Kasuga M, Yamaguchi-Shinozaki K, Carninci P, Hayashizaki Y, Shinozaki K: Monitoring the expression pattern of 1300 Arabidopsis genes under drought and cold stresses by using a full-length cDNA microarray. Plant Cell. 2001, 13: 61-72.PubMedPubMed CentralView ArticleGoogle Scholar
- Avonce N, Leyman B, Mascorro-Gallardo JO, Van Dijck P, Thevelein JM, Iturriaga G: The Arabidopsis trehalose-6-P synthase AtTPS1 gene is a regulator of glucose, abscisic acid, and stress signaling. Plant Physiol. 2004, 136: 3649-3659. 10.1104/pp.104.052084.PubMedPubMed CentralView ArticleGoogle Scholar
- Suzuki N, Bajad S, Shuman J, Shulaev V, Mittler R: The transcriptional co-activator mbf1c is a key regulator of thermotolerance in Arabidopsis thaliana. J Biol Chem. 2008, 283: 9269-9275. 10.1074/jbc.M709187200.PubMedView ArticleGoogle Scholar
- Bray EA: Plant responses to water deficit. Trends Plant Sci. 1997, 2: 48-54.View ArticleGoogle Scholar
- Nylander M, Svensson J, Palva ET, Welin BV: Stress-induced accumulation and tissue-specific localization of dehydrins in Arabidopsis thaliana. Plant Mol Biol. 2001, 45: 263-279. 10.1023/A:1006469128280.PubMedView ArticleGoogle Scholar
- Garay-Arroyo A, Colmenero-Flores JM, Garciarrubio A, Covarrubias AA: Highly hydrophilic proteins in prokaryotes and eukaryotes are common during conditions of water deficit. J Biol Chem. 2000, 275: 5668-5674. 10.1074/jbc.275.8.5668.PubMedView ArticleGoogle Scholar
- Medina J, Ballesteros ML, Salinas J: Phylogenetic and functional analysis of Arabidopsis RCI2 genes. J Exp Bot. 2007, 58: 4333-4346. 10.1093/jxb/erm285.PubMedView ArticleGoogle Scholar
- Buchanan C, Lim S, Salzman R, Kagiampakis I, Morishige D, Weers B, Klein R, Pratt L, Cordonnier-Pratt M, Klein P: Sorghum bicolor's transcriptome response to dehydration, high salinity and ABA. Plant Mol Biol. 2005, 58: 699-720. 10.1007/s11103-005-7876-2.PubMedView ArticleGoogle Scholar
- Wang D, Pan Y, Zhao X, Zhu L, Fu B, Li Z: Genome-wide temporal-spatial gene expression profiling of drought responsiveness in rice. BMC Genomics. 2011, 12: 149-163. 10.1186/1471-2164-12-149.PubMedPubMed CentralView ArticleGoogle Scholar
- Kasprzewska A: Plant chitinases–regulation and function. Cell Mol Biol Lett. 2003, 8: 809-824.PubMedGoogle Scholar
- Huang D, Wu W, Abrams SR, Cutler AJ: The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors. J Exp Bot. 2008, 59: 2991-3007. 10.1093/jxb/ern155.PubMedPubMed CentralView ArticleGoogle Scholar
- Varshney RK, Graner A, Sorrells ME: Genic microsatellite markers in plants: features and applications. Trends Biotechnol. 2005, 23: 48-55. 10.1016/j.tibtech.2004.11.005.PubMedView ArticleGoogle Scholar
- Nicot N, Chiquet V, Gandon B, Amilhat L, Legeai F, Leroy P, Bernard M, Sourdille P: Study of simple sequence repeat (SSR) markers from wheat expressed sequence tags (ESTs). Theor Appl Genet. 2004, 109: 800-805. 10.1007/s00122-004-1685-x.PubMedView ArticleGoogle Scholar
- Chang SJ, Puryear J, Cainey J: A simple and efficient method for RNA isolation from pine trees. Plant Mol Biol Rep. 1993, 11: 113-116. 10.1007/BF02670468.View ArticleGoogle Scholar
- Ewing B, Green P: Base-calling of automated sequencer traces using PHRED. II. Error probabilities. Genome Research. 1998, 8: 186-194.PubMedView ArticleGoogle Scholar
- Smith TF, Waterman MS: Identification of common molecular subsequences. J Mol Biol. 1981, 147: 195-197. 10.1016/0022-2836(81)90087-5.PubMedView ArticleGoogle Scholar
- Gotoh O: An improved algorithm for matching biological sequences. J Mol Biol. 1982, 162: 705-708. 10.1016/0022-2836(82)90398-9.PubMedView ArticleGoogle Scholar
- Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, Kawai K, Galbraith D, Bohnert HJ: Gene expression profiles during the initial phase of salt stress in rice. Plant Cell. 2001, 13: 889-905.PubMedPubMed CentralView ArticleGoogle Scholar
- Talame V, Ozturk NZ, Bohnert HJ, Tuberosa R: Barley transcript profiles under dehydration shock and drought stress treatments: a comparative analysis. J Exp Bot. 2007, 58: 229-240.PubMedView ArticleGoogle Scholar
- Gao C, Wang Y, Liu G, Yang C, Jiang J, Li H: Expression profiling of salinity-alkali stress responses by large-scale expressed sequence tag analysis in Tamarix hispid. Plant Mol Biol. 2008, 66: 245-258. 10.1007/s11103-007-9266-4.PubMedView ArticleGoogle Scholar
- Shi J, Liu M, Shi J, Zheng G, Wang Y, Wang J, Chen Y, Lu C, Yin W: Reference gene selection for qPCR in Ammopiptanthus mongolicus under abiotic stresses and expression analysis of seven ROS-scavenging enzyme genes. Plant Cell Rep. 2012, 31: 1245-1254. 10.1007/s00299-012-1245-9.PubMedView ArticleGoogle Scholar
- Temnykh S, DeClerck G, Lukashova A, Lipovich L, Cartinhour S, McCouch S: Computational and experimental analysis of microsatellites in rice (Oryza sativa L.): frequency, length variation, transposon associations, and genetic marker potential. Genome Res. 2001, 11: 1441-1452. 10.1101/gr.184001.PubMedPubMed CentralView ArticleGoogle Scholar
- Bräutigam M, Lindlöf A, Zakhrabekova S, Gharti-Chhetri G, Olsson B, Olsson O: Generation and analysis of 9792 EST sequences from cold acclimated oat, Avena sativa. BMC Plant Biol. 2005, 5: 18-34. 10.1186/1471-2229-5-18.PubMedPubMed CentralView ArticleGoogle Scholar
- Asp T, Frei UK, Didion T, Nielsen KK, Lübberstedt T: Frequency, type, and distribution of EST-SSRs from three genotypes of Lolium perenne, and their conservation across orthologous sequences of Festuca arundinacea, Brachypodium distachyon, and Oryza sativa. BMC Plant Biol. 2007, 7: 36-47. 10.1186/1471-2229-7-36.PubMedPubMed CentralView ArticleGoogle Scholar
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